Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-24 @ 5:13 PM
Ignite Modification Date:
2025-12-25 @ 2:51 PM
NCT ID:
NCT01981850
Group ID:
EG009
Title:
OLE Stage 2: RO7490677 10 mg/kg IV Q4W
Description:
Participants who completed 9 cycles of the originally assigned treatment could switch to the open label extension. Participants enrolled received PRM-151 at a dose of 10mg/kg Q4W on days 1, 3, and 5 of first cycle of the open label phase and Day 1 of each subsequent 28 day cycle.
Deaths Number Affected:
7
Deaths Number At Risk:
None
Serious Number Affected:
22
Serious Number At Risk:
48
Other Number Affected:
32
Other Number At Risk:
48
Study:
NCT01981850
Results Section:
NCT01981850
Adverse Events Module:
NCT01981850